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DCX - doublecortin
- Synonym(s) : DBCN, DC, doublecortex, LISX, SCLH, XLIS
- Previous symbols and names : doublecortex; lissencephaly, X-linked (doublecortin)
- Type : gene with protein product
- Chromosomal location : Xq23
- OMIM: 300121
- HGNC: 2714
- UniProtKB: O43602
- Genatlas: DCX
- GenCC: DCX
- Ensembl: ENSG00000077279
- IUPHAR-DB: -
- Reactome: O43602
- LOVD: DCX
Diseases list
- Disease-causing germline mutation(s) in Lissencephaly type 1 due to doublecortin gene mutation
ORPHA:2148 
- Disease-causing germline mutation(s) in Subcortical band heterotopia
ORPHA:99796
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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